Canonical Allele Identifier: PA2825851961
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818791
ClinVar RCV Id: RCV003625299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Pro31Thr
CA415076207
NM_001142805.2:c.91C>A